Variant #0000613627 (NC_000011.9:g.67164766_67164767insGC, NM_002708.3:c.*1239_*1240insGC (PPP1CA))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67164766_67164767insGC
DNA change (hg38) g.67397295_67397296insGC
Published as RAD9A(NM_001243224.1):c.761_762insGC (p.(Gln256ProfsTer66))
ISCN -
DB-ID PPP1CA_000004
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-01 09:42:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP1CA NM_002708.3 -?/. - c.*1239_*1240insGC r.(=) p.(=)
RAD9A NM_004584.2 -?/. - c.989_990insGC r.(?) p.(Gln332ProfsTer66)


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